Pharmacological characterization of a fluorescent uptake assay for the noradrenaline transporter

J Biomol Screen. 2007 Apr;12(3):378-84. doi: 10.1177/1087057107299524. Epub 2007 Mar 22.

Abstract

The noradrenaline transporter (NET) is a Na(+)/Cl(-) dependent monoamine transporter that mediates rapid clearance of noradrenaline from the synaptic cleft, thereby terminating neuronal signaling. NET is an important target for drug development and is known to be modulated by many psychoactive compounds, including psychostimulants and antidepressants. Here, the authors describe the development and pharmacological characterization of a nonhomogeneous fluorescent NET uptake assay using the compound 4-(4-dimethylaminostyryl)-N-methylpyridinium (ASP(+)). Data presented show that the pharmacology of both the classic radiolabeled (3)H-noradrenaline- and ASP(+)-based uptake assays are comparable, with an excellent correlation between potency obtained for known modulators of NET (r = 0.95, p < 0.0001). Furthermore, the fluorescent uptake assay is highly reproducible and has sufficiently large Z' values to be amenable for high-throughput screening (HTS). The advantage of this assay is compatibility with both 96- and 384-well formats and lack of radioactivity usage. Thus, the authors conclude that the assay is an inexpensive, viable approach for the identification and pharmacological profiling of small-molecule modulators of the monoamine transporter NET and may be amenable for HTS.

MeSH terms

  • Animals
  • Biological Assay / methods*
  • Dogs
  • Dose-Response Relationship, Drug
  • Fluorescent Dyes / analysis
  • Fluorescent Dyes / metabolism*
  • Humans
  • Kinetics
  • Norepinephrine Plasma Membrane Transport Proteins / metabolism*
  • Psychotropic Drugs / pharmacology
  • Pyridinium Compounds / pharmacology*
  • Tritium

Substances

  • 4-(4-dimethylaminostyryl)-1-methylpyridinium
  • Fluorescent Dyes
  • Norepinephrine Plasma Membrane Transport Proteins
  • Psychotropic Drugs
  • Pyridinium Compounds
  • Tritium